Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.08 (G)

Chromosome 1:161230796 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs59634807, rs17397854

HGVS names

This variant has 33 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 45 transcripts, has 3761 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays